A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739262



Internal ID162928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11707246..11713279hg38UCSC Ensembl
chrX:11725366..11731399hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386034
hg196034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739262
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.319019


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